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J Biol Chem, Vol. 273, Issue 7, 4135-4142, February 13, 1998

Kidney Injury Molecule-1 (KIM-1), a Putative Epithelial Cell Adhesion Molecule Containing a Novel Immunoglobulin Domain, Is Up-regulated in Renal Cells after Injury

Takaharu IchimuraDagger , Joseph V. BonventreDagger , Véronique Bailly, Henry Wei, Catherine A. Hession, Richard L. Cate, and Michele Sanicola

From the Dagger  Renal Unit, Medical Services, Massachusetts General Hospital East and the Department of Medicine, Harvard Medical School, Boston, Massachusetts 02129, and  Biogen Incorporated, Cambridge, Massachusetts 02142

We report the identification of rat and human cDNAs for a type 1 membrane protein that contains a novel six-cysteine immunoglobulin-like domain and a mucin domain; it is named kidney injury molecule-1 (KIM-1). Structurally, KIM-1 is a member of the immunoglobulin gene superfamily most reminiscent of mucosal addressin cell adhesion molecule 1 (MAdCAM-1). Human KIM-1 exhibits homology to a monkey gene, hepatitis A virus cell receptor 1 (HAVcr-1), which was identified recently as a receptor for the hepatitis A virus. KIM-1 mRNA and protein are expressed at a low level in normal kidney but are increased dramatically in postischemic kidney. In situ hybridization and immunohistochemistry revealed that KIM-1 is expressed in proliferating bromodeoxyuridine-positive and dedifferentiated vimentin-positive epithelial cells in regenerating proximal tubules. Structure and expression data suggest that KIM-1 is an epithelial cell adhesion molecule up-regulated in the cells, which are dedifferentiated and undergoing replication. KIM-1 may play an important role in the restoration of the morphological integrity and function to postischemic kidney.


Copyright © 1998 by The American Society for Biochemistry and Molecular Biology, Inc.

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